Canonical Allele Identifier: CA10650294

Gene: TP53 WRAP53

Linked Data

• ClinVar Variation Id: 325646
• ClinVar RCV Id: RCV000272984 ; RCV001126970
• dbSNP Id: rs886053516
• MyVariant Identifiers: chr17:g.7590768G>C (hg19) ; chr17:g.7687450G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7687450G>C , CM000679.2:g.7687450G>C	GRCh38
NC_000017.10:g.7590768G>C , CM000679.1:g.7590768G>C	GRCh37
NC_000017.9:g.7531493G>C	NCBI36
NG_017013.2:g.5101C>G , LRG_321:g.5101C>G
NG_028245.1:g.6380G>C , LRG_375:g.6380G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509690.6:c.-95C>G (TP53)	ENSP00000425104.2:n.-95C>G
ENST00000571370.2:n.74C>G (TP53)
ENST00000604348.6:c.-102C>G (TP53)	ENSP00000473895.2:n.-102C>G
ENST00000269305.9:c.-102C>G (TP53) MANE Select	ENSP00000269305.4:n.-102C>G
ENST00000269305.8:c.-102C>G (TP53)	ENSP00000269305.4:n.-102C>G
ENST00000316024.9:c.-1199G>C (WRAP53)	ENSP00000324203.5:n.-1199G>C
ENST00000420246.6:c.-102C>G (TP53)	ENSP00000391127.2:n.-102C>G
ENST00000431639.6:c.-1-1198G>C (WRAP53)	ENSP00000397219.2:n.-1-1198G>C
ENST00000445888.6:c.-99C>G (TP53)	ENSP00000391478.2:n.-99C>G
ENST00000455263.6:c.-102C>G (TP53)	ENSP00000398846.2:n.-102C>G
ENST00000457584.6:c.-155G>C (WRAP53)	ENSP00000411061.2:n.-155G>C
ENST00000505014.5:n.38C>G (TP53)
ENST00000509690.5:c.-95C>G (TP53)	ENSP00000425104.1:n.-95C>G
ENST00000604348.5:c.-102C>G (TP53)	ENSP00000473895.1:n.-102C>G
ENST00000610292.4:c.-336C>G (TP53)	ENSP00000478219.1:n.-336C>G
ENST00000610538.4:c.-219C>G (TP53)	ENSP00000480868.1:n.-219C>G
ENST00000617185.4:c.-102C>G (TP53)	ENSP00000482258.1:n.-102C>G
ENST00000619485.4:c.-216C>G (TP53)	ENSP00000482537.1:n.-216C>G
ENST00000620739.4:c.-219C>G (TP53)	ENSP00000481638.1:n.-219C>G
ENST00000622645.4:c.-219C>G (TP53)	ENSP00000482222.1:n.-219C>G
ENST00000635293.1:c.-219C>G (TP53)	ENSP00000488924.1:n.-219C>G
NM_000546.5:c.-102C>G , LRG_321t1:c.-102C>G (TP53)	NP_000537.3:n.-102C>G
NM_001126112.2:c.-99C>G , LRG_321t2:c.-99C>G (TP53)	NP_001119584.1:n.-99C>G
NM_001126113.2:c.-102C>G , LRG_321t4:c.-102C>G (TP53)	NP_001119585.1:n.-102C>G
NM_001126114.2:c.-102C>G , LRG_321t3:c.-102C>G (TP53)	NP_001119586.1:n.-102C>G
NM_001126118.1:c.-336C>G , LRG_321t8:c.-336C>G (TP53)	NP_001119590.1:n.-336C>G
NM_001143990.1:c.-1-1198G>C (WRAP53)	NP_001137462.1:n.-1-1198G>C
NM_001143991.1:c.-155G>C (WRAP53)	NP_001137463.1:n.-155G>C
NM_001276695.1:c.-219C>G (TP53)	NP_001263624.1:n.-219C>G
NM_001276696.1:c.-219C>G (TP53)	NP_001263625.1:n.-219C>G
NM_001276760.1:c.-219C>G (TP53)	NP_001263689.1:n.-219C>G
NM_001276761.1:c.-216C>G (TP53)	NP_001263690.1:n.-216C>G
NM_001143991.2:c.-155G>C (WRAP53)	NP_001137463.1:n.-155G>C
NM_001276695.2:c.-219C>G (TP53)	NP_001263624.1:n.-219C>G
NM_001276696.2:c.-219C>G (TP53)	NP_001263625.1:n.-219C>G
NM_001276760.2:c.-219C>G (TP53)	NP_001263689.1:n.-219C>G
NM_001276761.2:c.-216C>G (TP53)	NP_001263690.1:n.-216C>G
NM_000546.6:c.-102C>G (TP53) MANE Select	NP_000537.3:n.-102C>G
NM_001126112.3:c.-99C>G (TP53)	NP_001119584.1:n.-99C>G
NM_001126113.3:c.-102C>G (TP53)	NP_001119585.1:n.-102C>G
NM_001126114.3:c.-102C>G (TP53)	NP_001119586.1:n.-102C>G
NM_001126118.2:c.-336C>G (TP53)	NP_001119590.1:n.-336C>G
NM_001143990.2:c.-1-1198G>C (WRAP53)	NP_001137462.1:n.-1-1198G>C
NM_001276695.3:c.-219C>G (TP53)	NP_001263624.1:n.-219C>G
NM_001276696.3:c.-219C>G (TP53)	NP_001263625.1:n.-219C>G
NM_001276760.3:c.-219C>G (TP53)	NP_001263689.1:n.-219C>G
NM_001276761.3:c.-216C>G (TP53)	NP_001263690.1:n.-216C>G